Product Details

SNP ID
rs143532619
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:27614524 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCGCTCCCCAACCAGGATGTTGGC[C/T]GCCCTCAGGTCGCGGTGAATGTAGT
Phenotype
MIM: 164940
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FGR PubMed Links

Gene Details

Gene
FGR
Gene Name
FGR proto-oncogene, Src family tyrosine kinase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001042729.1 1383 Silent Mutation GCA,GCG A385A NP_001036194.1
NM_001042747.1 1383 Silent Mutation GCA,GCG A385A NP_001036212.1
NM_005248.2 1383 Silent Mutation GCA,GCG A385A NP_005239.1
XM_006710452.2 1383 Silent Mutation GCA,GCG A385A XP_006710515.1
XM_011541010.1 1383 Silent Mutation GCA,GCG A385A XP_011539312.1
XM_011541011.2 1383 Silent Mutation GCA,GCG A316A XP_011539313.1
XM_011541012.1 1383 Intron XP_011539314.1
XM_011541013.2 1383 Intron XP_011539315.1
XM_011541014.2 1383 Silent Mutation GCA,GCG A181A XP_011539316.1
XM_017000673.1 1383 Silent Mutation GCA,GCG A181A XP_016856162.1
XM_017000674.1 1383 Silent Mutation GCA,GCG A181A XP_016856163.1

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